Canonical Allele Identifier: PA2741906337
Gene: CRADD HGNC NCBI

Linked Data

ClinVar Variation Id: 2722687
ClinVar RCV Id: RCV003559018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003796.1:p.Arg168Trp
CA6720242
NM_003805.5:c.502C>T